Conditional deletion of cytochrome p450 reductase in osteoprogenitor cells affects long bone and skull development in mice recapitulating antley-bixler syndrome: role of a redox enzyme in development (Q35005855)

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English	Conditional deletion of cytochrome p450 reductase in osteoprogenitor cells affects long bone and skull development in mice recapitulating antley-bixler syndrome: role of a redox enzyme in development	scientific article

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Europe PubMed Central

PubMed publication ID

5 August 2017

Conditional deletion of cytochrome p450 reductase in osteoprogenitor cells affects long bone and skull development in mice recapitulating antley-bixler syndrome: role of a redox enzyme in development (English)

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5 August 2017

Antley-Bixler syndrome

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Srikanth R Polusani

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Srikanth R Polusani

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Satya P Panda

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5 August 2017

Anyonya R Guntur

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5 August 2017

Roberto J Fajardo

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5 August 2017

Peter T Gakunga

5

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5 August 2017

Linda J Roman

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5 August 2017

Bettie Sue Masters

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5 August 2017

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25 September 2013

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Europe PubMed Central

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5 August 2017

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5 August 2017

8

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5 August 2017

9

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5 August 2017

e75638

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Europe PubMed Central

PubMed publication ID

5 August 2017

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Creative Commons Attribution 4.0 International

25 September 2013

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3783497/fullTextXML

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Genetic and molecular control of osterix in skeletal formation

1 reference

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Neurobehavioral abnormalities in a brain-specific NADPH-cytochrome P450 reductase knockout mouse model

1 reference

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ERK acts in parallel to PKCδ to mediate the connexin43-dependent potentiation of Runx2 activity by FGF2 in MC3T3 osteoblasts

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Building strong bones: molecular regulation of the osteoblast lineage

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Ugonin K promotes osteoblastic differentiation and mineralization by activation of p38 MAPK- and ERK-mediated expression of Runx2 and osterix

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Regulation of gap junction function and Connexin 43 expression by cytochrome P450 oxidoreductase (CYPOR).

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Mouse knockout of the cholesterogenic cytochrome P450 lanosterol 14alpha-demethylase (Cyp51) resembles Antley-Bixler syndrome

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Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

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Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPH-cytochrome P450 oxidoreductase

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10.1371/JOURNAL.PONE.0075638

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Europe PubMed Central

PubMed publication ID

5 August 2017

2013PLoSO...875638P

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Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

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Europe PubMed Central

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5 August 2017

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